Algicidal dihalomethylglutaronitriles

ABSTRACT

Antimicrobial 2-halo-2-halomethylglutaronitriles are prepared by the halogenation of 2-methyleneglutaronitrile.

United States Patent 1 Grier et al.

[ ALGICIDAL DIHALOMETHYLGLUTARONITRILES [75] Inventors: Nathaniel Grier, Englewood;

Seymour J. Lederer, Fair Lawn, both of NJ.

[52] U.S. Cl 71/67; 424/304 [51] Int. Cl A01n 9/20 [58] Field of Search 71/67 Apr. 15, 1975 [56] References Cited UNITED STATES PATENTS 2,419,021 4/1947 Harnden 71/67 3,644,463 2/1972 Parke 71/67 3,764,291 10/1973 Barker 71/67 Primary Examiner-Lewis Gotts Assistant Examiner-Catherine L. Mills Attorney, Agent, or Firm-Edmunde D. Riedl; .1. Jerome Behan; Frank M. Mahon [57] ABSTRACT .Antimicrobial 2-halo-2-halomethylglutaronitriles are prepared by the halogenation of 2- methyleneglutaronitrile.

1 Claim, No Drawings ALGICIDAL DIHALOMETHYLGLUTARONITRILES This is a division of application Ser. No. 102,197, filed Dec. 28, 1970.

This invention relates to new compositions of matter useful in agricultural and in industrial applications as antimicrobial agents (fungicidal, bactericidal and algicidal). More particularly, the instant invention relates to antimicrobial compositions containing, as the essential active ingredient, a 2-halo-2- halomethylglutaronitrile and to processes for employing such compositions as antimicrobials in agricultural and industrial applications.

Fields of technology adversely affected by fungal, bacterial and algal growth are many and include, for example, the paint, wood, textile, cosmetic, leather, tobacco, fur, rope, paper, pulp, plastics, fuel, oil, and rubber industries. Fungicides and bactericides are also utilized for agricultural applications such as, for instance, in preventing or minimizing the growth of harmful fungi and/or bacteria on plants, trees, fruits, seeds or soil. The instant invention is based upon the discovery that the 2-halo-2-halomethylglutaronitriles described hereinafter are effective antimicrobials when employed in these and in other applications.

As used in the description of this invention, the expressions antimicrobial, fungicide," bactericide, algicide" and the like are intended to encompass control of fungi, bacteria (both aerobic and anaerobic) and algae broadly and to include the killing as well as inhibiting the growth of such organisms.

In its composition aspect, therefore, the instant invention may be described as residing in the concept of antimicrobial compositions containing as the essential active ingredient an antimicrobially effective quantity of a 2-halo-2-halomethylglutaronitrile of the formula:

CH X

NC (i3 CH CH CN wherein X is a member selected from the group consisting of chlorine and bromine. It is contemplated that antimicrobial formulations containing an effective amount of such 2-halo-2-halomethylglutaronitriles will be employed as antimicrobial agents in industrial and agricultural applications.

As noted above, the instant invention is based upon the discovery that the 2-halo-2- halomethylglutaronitriles described above are effective in controlling the growth of bacteria, fungi and algae in a variety of industrial and agricultural applications. It has been found, for example, that these compounds are effective antimicrobials for the destruction or control of soil fungi and bacteria and for the protection of seeds, bulbs and plants. Also they are effective algicides in the treatment of pools and ponds, cooling water systems and the like. The utility of the 2-halo-2- halomethylglutaronitriles of this invention is shown not only by their activity against bacteria and fungi responsible for stunting growth, and even destruction of many types of crop-producing plants, but also for those causing degradation and deterioration of many types of industrial products including, for example, paper, leather, textiles, aqueous systems such as adhesives, resins, drilling fluids, pigment dispersions and latex paints and oleoresinous coatings whose films are particularly vulnerable to the destructive action of fungi. The large economic losses encountered in paper-making operations caused by the accumulation of bacterial and fungal slimes in various parts of the system can be eliminatd to a significant extend by the use of the compounds described herein.

The antimicrobial activity of the compounds described above has been confirmed using standard labo' ratory techniques. They have been found effective, for example, in inhibiting bacteria including Aerobacter sp. such as A. aerogenes, Bacillus sp. such B. mycoides Pseudomonas sp. such as P. aeruginosa, Staphylococcus sp. such as S. aureus, Escherichia sp. such as E. coli, Cellulomonas sp. such as C. hiazotea, Proteus sp. such as P. mirabilis and sulfate reducing bacteria including Desulfovibrio sp., such as D. desulfuricans. They have been found effective also against fungi including Rhodotorula sp., Alternaria sp., Aspergillus sp. such as A. niger, Pullularia sp. such as P. pullulans, Penicillium sp. such as P. luteum, Chaetomium sp. such as C. globusum, Trichoderma sp. such as T. viride, Rhizoctonia sp. such as R. .s'olani. Such bacteria and/or fungi commonly are found on cereal and grain products; on oils, on fruits and vegetables and on cosmetics, leather, electrical insulation, textiles and numerous other materials capable of supporting their growth. Also, such bacteria and/or fungi may be found on plants, seeds, fur and wood and in soils. Further, they may be used to control overgrowth of algae such as Chlorella sp. including C. pyrenoidosa.

The 2-halo-2-halomethylglutaronitriles of this invention, conveniently, may be prepared from 2- methyleneglutaronitrile, a compound commercially available, by halogenation. The halogenation may be effected by intimately contacting the 2- methyleneglutaronitrile with halogen, chlorine or bromine, preferably at temperatures below about 30C. and in the absence of a solvent. The addition of halogen to the reaction mixture is continued until an equimolar quantity of halogen is absorbed which usually requires from about 8 to about 72 hours. Where the 2-halo-2- halomethyl glutaronitrile so formed is a liquid, it may be purified by distillation under reduced pressure. If solid, the product may be recovered by solvent extraction followed by evaporation of the solvent and conventional recrystallization of the crude residue.

Alternatively, the halogenation of the 2- methyleneglutaronitrile may be carried out in the presence of a suitable organic solvent such as methylene chloride, hexane, benzene, carbon disulfide, carbon tetrachloride, ethyl acetate and the like. The reaction usually is carried out with the reaction temperature maintained below about 30C. using external cooling. Upon absorption of an equimolar quantity of halogen, the reaction products may be recovered as indicated above.

It will be understood that the 2-halo-2- halomethylglutaronitriles described above may be used in diverse formulations, solid, including finely divided powders and granular materials as well as liquid, such as solutions, emulsions, suspensions, concentrates, emulsifiable concentrates, slurries and the like, depending upon the application intended and the formulation media desired. Further, when the 2-halo-2- methylglutaronitrile is liquid, it may be employed neat or may be incorporated into various formulations, both solid and liquid, as an adsorbate on suitable inert carriers such as talc, clays, diatomaceous earth and the like.

Thus, it will be appreciated that the 2-halo-2- halomethylnitrile may be employed to form antimicrobial formulations containing such compounds as the essential active ingredient, which formulations may also contain a variety of carrier materials adaptable to industrial and agricultural applications including finely divided dry or liquid diluents, extenders, clays, diatomaceous earth, talc and the like, or water and various organic liquids such as loweralkanols, kerosene, benzene, toluene and other petroleum distillate fractions or mixtures thereof.

It will be understood also that the active 2-halo-2- halomethylglutaronitriles described above may beused in combination one with the other as well as with other antimicrobial materials. For example, these compounds can be combined with other fungicides and bactericides such as 2-(4-thiazolyl)benzimidazole, sorbic acid, propionic acid, mycostatin, sodium diacetate, trichomycin, amphotericin, griseofulvin, undecylenic acid, esters of parahydroxybenzoic acid, chlorquinaldol, 5,7-dichloro-8hydroxyquinoline, sodium-- phenylphenate, o-phenylphenol, biphenyl chlorinated phenols, sodium benzoate in appropriate concentrations and in appropriate instances so as to combine the action of each to obtain particularly useful results. Such combinations might find particular application in the preparation of germicidal soaps, in the production of cosmetics and aqueous coatings and in combatting paper mill slime accumulations. It is quite clear also that the 2-halo-2-halomethyl glutaronitriles can be combined with other algicidal agents such as benzalkonium chlorides and other quaternary ammonium compounds to obtain formulations particularly suitable to special problems of algae control.

As noted above, it has been found that growth of various harmful fungi and bacteria existing in soil is eliminated or limited by use of formulations containing the 2-halo-2-halomethylglutaronitriles described herein. The term, soil, as used here is intended to include all media capable of supporting growth of plants and may include humus, sand, manure, compost, artifically created plant growth solutions and the like.

The 2-halo-2-halomethylglutaronitriles described above have activity against bacteria, fungi and algae when employed at appropriate levels of concentration and may be used to inhibit growth of these organisms. It will be obvious to those skilled in the art that the required effective concentration will vary with particular organisms and in particular applications. In general, however, effective fungicidal, bactericidal and algicidal response is obtained when the 2-halo-2- halomethylglutaronitriles are employed in concentrations ranging between 0.5 and 1000 ppm. (parts per million).

The best mode contemplated by applicants for carrying out their invention is more fully illustrated in the following examples; no limitation however, being intended except as set forth in the appended claims.

EXAMPLE 1 2Chloro-2chloromethylglutaronitrile Place 106 gm. of 2methyleneglutaronitrile in a flask fitted with a stirrer, a calcium chloride drying tube and a subsurface gas inlet tube. Cool to l520C. and add chlorine gas with agitation at such rate that the temperature does not exceed 20C. When an equimolar quantity of chlorine is absorbed, cease addition of chlorine gas and continue stirring for an additional hour. Purify the product by distillation under reduced pressure to obtain 2-chloro-2-chloromethylglutaronitrile (b.p. 136l38 at 1.5 mm).

EXAMPLE 2 2-Bromo-2-bromomethylglutaronitrile Combine 106 gm of 2-methyleneglutaronitrile and 160 gm of liquid bromine and stir at a temperature of 2527C. for 72 hours. Treat the reaction mixture with aqueous sodium bisulfite and extract with three ml. portions of ethyl ether. Wash the ether extracts with three 50 ml. portions of aqueous sodium bicarbonate and dry with anhydrous magnesium sulfate. Remove the magnesium sulfate by filtration and evaporate the ether. Purify the crude residue by recrystallization from isopropanol to obtain 2-bromo-2- bromomethylglutaronitrile. (m.p. 51.252.5C.)

EXAMPLE 3 2-Bromo-2bromomethylglutaronitrile Add 424.5 gm. of 2-methyleneglutaronitrile in 400 ml. of methylene chloride to a 3 l., 3-neck round bottom flask equipped with stirrer, thermometer, condenser and dropping funnel. Add 639.3 gm. of bromine in 400 ml. of methylene chloride to the dropping funnel. Cool the methyleneglutaronitrile solution with stirring to 15C. on an ice bath. Add bromine solution dropwise to reaction flask over approximately 1.5 hours maintaining reaction temperature at l520C. Age with stirring at 20C. for 3 hours and continue stirring at room temperature for 60-70 hours. Distill off solvent under vacuum at about 40C. maintaining constant volume by continual addition of ethanol. Cool alcohol solution to 4C. and separate product by filtration. Wash filter cake with cold alcohol and dry under vacuum. Recrystallize from ethanol to obtain Z-bromo- 2bromomethylglutaronitrile.

EXAMPLE 4 In order to determined antimicrobial spectrum, the

following techniques are employed:

Antibacterial Activity A stock solution of the sample to be tested is prepared in 25% methanol. Dilutions of the stock solution are made into Tryptone Glucose Extract Agar (Difco) and the agar is poured into sterile petri dishes. After hardening, the plates are streaked with an aqueous suspension of the test organism. The inoculated plates are incubated at 3537C. and examined after 24 hours for the presence or absence of growth. The lowest concentration at which no growth occurred is reported as the, Inhibiting Concentration.

Antifungal Activity A stock solution of the sample to be tested is prepared in 25% methanol. Dilutions of the stock solution are made into Sabouraud Maltose Agar (Difco) and the agar is poured into sterile petri dishes. After hardening, the plates are streaked with an aqueous spore suspension of the test organism. No wetting agent is used in preparation of the suspension. The inoculated plates are incubated at 2830C. and examined after seven days for the presence or absence of growth. The lowest concentration at which no growth occurred, is reported as the, Inhibiting Concentration.

Employing the techniques described above, 2-

TAPPl Standard Sulfite Pulp 0.05% Technical Association of the Pulp and Paper Industry,

New York, New York bromo-2-bromomethylglutaronitrile was tested at l, 5 Trypticase Soy Broth, Sterile 0.05% 10, 50 and 100 ppm against the organisms, and with the Saturated Alum Solution to pH 4.5 results, indicated in the following table. Aerobacter aerogenes suspension 0.1%.

TABLE I Aliquots (100 ml.) of the white water are placed in oversized containers suitable for use on a shaker (e.g. INHIBITING 10 bottles, flasks). Test compound is added to these ali- CONCENTRATION quots to produce the desired test concentrations. An ORGANISM (PPM) uninhibited control is included in each test. Plate Bacteria: Aembamr aemgenes 50 counts are run on the uninhibited at zero time and on Bacillus mycoides 10 the treated aliquots at 1 hour, 4 hours and 24 hours Pswdmwm 50 after the start of the test. The percentage reduction in Staphylococcus aureus 50 Escherichia 10 the count for each inhibitor level and at each time inge ul 171 m terval is calculated by comparing the bacterial popula- TOIEIAS mtra llS Fungi, succhummyces 50 tion of each sample with that of the uninhibited con- Rhvdvwrulfl SP- 100 trol. To be considered of value the percent reduction jig fgg 's gg achieved by the test compound must be at least 90%, Pullularia pullulans 100 and preferably 99%, within 4 hours. The results of this Penicillium luleum 100 experiment using 2 b 2 Chaetomium glohosum 100 Triclmderma \iride 100 bromomethylglutaronitrile are summarized n the fol- Rhizocmnia solani 50 l i bl TABLE III CONCENTRA- REDUCTION (7:)

TlON COMPOUND (PPM) 1 hr. 4 hr. 24 hr.

2-Bromo-2-bromomethyl- 50 99.99 99.99 99.99 glutaronitrile 25 99.99 99.99 99.99 10 99.0 99.9 99.99 99.0 99.99 CONTROL (Bacteria/ml.) 49x10 LIXlO" 3 10 EXAMPLE 5 EXAMPLE 7 2-Bromo-2-bromomethylglutaronitrile was tested for Th ffl f 2 b 2 its bactericidal activity of the time-kill method. The test consists of inoculating a culture of Aerobacter aerogenes into sterile water, adding known concentrations of the test chemical, and allowing the two to remain in contact for a known period of time. Bacterial counts are run after the alloted contact time. The effectiveness of the test chemical is determined by comparing the counts to a control count containing only sterile water and the bacteria taken at 0 hours. Results of the test are summarized in the following table.

bromomethylglutaronitrile as a paper mill slime control agent was evaluated by the following technique.

An artificial paper mill white water is prepared consisting of the following in tap water:

bromomethylglutaronitrile as a preservative for paints during storage, both alone and in the presence of an added mildewcide, 2-(4'-thiazo1yl)benzimidazole, was evaluated by the following method.

Exterior polyvinyl acetate and interior acrylic paints having the formulas indicated in TABLES IV and V were prepared for testing.

Aliquots of each paint sample are placed in sterile containers. Each sample is streaked on the surface of plates of Tryptone Glucose Extract Agar (TGE) to check its bacterial condition. Bacteria free samples are then inoculated with a twenty-four hour old broth culture of Pseudomonas aeruginosa ATCC 10145 (American Type Culture Collection) at the rate of 1 ml. of culture per gm. of sample. The inoculated samples are incubated at 2830C. The microbiological condition of each sample is checked after 24, 48, 72 hours and seven days by streaking on the surface of TGE plates. These plates are incubated at 2830C. for 7 days and examined for growth. Seven days after the first inoculation samples are reinoculated with P. aeruginosa ATCC 10145 and streaked on TGE at 24, 48, 72 hours and seven days after reinoculation. Samples which achieve sterility within 48 hours after inoculation and reinoculation, and which are still sterile seven days after inoculation and reinoculation, are considered to be adequately preserved. The results achieved with the test samples indicated above are summarized in TABLE VI.

TABLE IV PVA EXTERIOR (COMPOSITION PARTS BY WEIGHT) COWLES DISPERSER l 2 3 4 6 7 8 9 Water 140 140 140 140 140 140 140 140 140 I Daxed 30 Na Salt of Polymerized Carboxylic Acid W. R. Grace Co. 6 6 6 6 6 6 6 6 6 6 Potassium Tripolyphosphate l l I I 1 1 1 1 1 1 Igepul C0-630 Nonylphenoxypoly-(ethylencoxy)ethanol General Aniline & Film Co. 1.5 1.5 1.5 1.5 1.5 1.5 1.5 L5 1.5 1.5 Polyethyleneglycol 2 2 2 2 2 2 2 2 2 2 Methylccllulose Solution (3%) 70 70 70 70 70 70 70 70 70 Defoamer 1 I I l 1 1 l l l 1 2 Brom0-2-bromomethylglutaronitrile 0 1.1 2.75 1.1 0.55 0.825 0.0275 0.55 0.825 l.I (DBGN) (0.1%) (0.25%) (0.1%) (0 05%) (0.075%) (0.025%) (0.05%) (0.05%) (0.1%) 2(4'Thiazolyl)benzimiduzole 0 1.1 1.1 2.75 2.75 2.75 0 0 0 O (TBZ) (0.1%) (0.1%) (0.25%) (0.25%) (0.25%) Titanium Dioxide 250 250 250 250 250 250 250 250 250 250 DISPERSE TEN MINUTES AT 4800 RPM Talc 75 75 75 75 75 75 75 75 75 DISPERSE TEN MINUTES AT 4800 RPM REDUCTION Methylcellulose Solution (3%) 68.5 68.5 68.5 68.5 68.5 68.5 68.5 68.5 68.5 68.5 Methyl C urbitol 20 20 20 20 20 20 20 20 20 20 Ethylene Glycol 40 40 40 40 40 40 40 40 40 4O Polyvinyl Acetate Emulsion 425 425 425 425 425 425 425 425 425 425 TABLE V INTERIOR ACRYLIC (COMPOSITION PARTS BY WEIGHT) COWLES DISPERSER l 2 3 4 5 6 7 8 9 10 Water 450 450 450 450 450 450 450 450 450 450 Diethylene Glycol 30 30 30 30 30 30 30 30 30 30 Methylcellulose 4000 cps 5 5 5 5 5 5 5 5 5 5 Potassium Tripolyphosphate 1.66 1.66 1.66 1.66 1.66 1.66 1.66 1.66 1.66 1.66 Lecithin 4 4 4 4 4 4 '4 v 4 4 4 Defoumer 3 3 3 3 3 3 3 3 3 3 2-Bromo-2-brom0methylglutaro- 0 1.08 2.7 1.08 0.54 0.81 0.27 0.54 0.81 1.08 nilrilc (DBGM) (0.1%) (0.25%) (0.1%) (0.05%) (0.075%) 0 025%) (0.05%) (0.075%) (0.1%) 2-( 4'-Thiazolyl )benzimidazole 0 1.08 1.08 2.7 2.7 2.7 0 0 0 0 (TBZ) (0.1%) (0.1%) (0.25%) (0.25%) (0.25%) Titanium Dioxide I25 125 125 125 125 I25 125 125 125 DISPERSE TEN MINUTES AT 4800 RPM TALC 250 250 250 250 250 250 250 250 250 250 Calcium Silicate 5 5 5 5 5 5 5 5 5 5 DISPERSE TEN MINUTES AT 4800 RPM REDUCTION Acrylic Resin Emulsion 208 208 208 208 208 208 208 208 208 208 PREMIX DIETHYLENE GLYCOL AND METHYLCELLULOSE PRIOR TO ADDING TO WATER TABLE VI TIME WITHIN WHICH STERILITY ATTAINED (HRS.)

PVA ACRYLIC SAMPLE DBGN% TBZ% INOCULATION REINOCU- INOCULATION REINOCULA- NO LATION TION 7 0.025 0 48 48 24 72 8 0.05 0 48 48 24 24 9 0.075 0 24 24 24 24 10 0.1 0 24 24 24 24 5 0.05 0.25 24 24 24 24 6 0.075 0.25 '24 24 24 24 4 0.1 0.25 24 24 24 24 2 0.1 0.1 24 24 24 24 3 0.25 0.1 24 24 4 4 l 0 O COMPLETE DEGRADATION DBGN Z-Bromo-2-hromomethylglularcnitrilc "TBZ 2-(4'-Thiazolyl )bcnzimidazolc EXAMPLE 8 Z-Bromo-2-bromomethylglutaronitrile was testes for aligicidal properties employing the following technique:

An actively growing culture of Chlorella sp. is prepared in a modified Allens Liquid Media. Varying concentrations of the chemical to be tested are added to 50 ml. portions of the culture. Each sample then is incubated at 22C. for 2 weeks. Each sample during the test period is illuminated with a fluorescent lamp source providing 50 foot candles at base of each flask. The lamp is on 16 hours and off 8 hours during each day of the incubation period. At the end of the test period, each sample is examined microscopically for algae growth. The results of this experiment are summarized in the following table.

TABLE Vll DBGN *CONCENTRATION M lCROSCOPlC (PPM) EXAMlNATlON 3000 All cells dead 2000 All cells dead l000 All cells dead 800 All cells dead 600 All cells dead 400 All cells dead 200 50% Cells dead 50% same as control *DBGN Z-Hromo-Z-bromumcthylgluluronitrilc EXAMPLE 9 ommended Practice for Biological Analysis of Subsurface lnjection Waters.

Fresh Water Brine For tests in brine the nutrient medium and assay medium are modified by the addition of sodium chloride to give an appropriate chloride concentration of 15,000 ppm.

The results of this experiment are summarized in the following table:

TABLE Vlll DBGN* CONCENTRATlON (PPM) FRESH WATER BRINE 50 No Growth No Growth 25 Ferrous Sulfide No Growth Visible l0 Ferrous Sulfide No Growth Visible 5 Ferrous Sulfide Ferrous Sulfide Visible Visible l Ferrous Sulfide Ferrous Sulfide Visible Visible *DBGN 2-Brumo-2-hromumethylgluluronilrile What is claimed is:

l. The method of controlling the growth of algae which comprises contacting the area upon which the growth of algae is to be controlled with an algicidally effective amount of 2-brom0-2- bromomethylglutaronitrile. 

1. THE METHOD OF CONTROLLING THE GROWTH OF ALGAE WHICH COMPRISES CONTACTING THE AREA UPON WHICH THE GROWTH OF ALGAE IS TO BE CONTROLLED WITH AN ALGICIDALLY EFFECTIVE AMOUNT OF 2BROMO-2-BROMOMETHYLGLUTARONITRILE. 